Infantile spasms are a type of epilepsy with a characteristic age of onset (typical age when seizures start), pattern of seizures and electroencephalogram (EEG). This means that it is an ‘electroclinical epileptic syndrome’.
They can also be called ‘salaam spasms’, because the appearance of the seizures is like a bowing forwards or backwards movement, or ‘West syndrome’ after Dr West who first described the condition in his own four month old son in 1841.
This type of epilepsy occurs in about one in 3000 children. Every year in the UK about 350-400 children will develop West syndrome.
Symptoms
In nine out of 10 children with the condition, infantile spasms occur in the first year of life, typically between three and eight months old. Often, to begin with, the attacks are brief, infrequent and not typical of the syndrome, so it is quite common for the diagnosis to be made late. Frequently, because of the pattern of attacks and the cry that a child gives during or after an attack, they are initially thought to be colic.
The typical pattern is of a sudden flexion (bending forward) in a tonic (stiffening) fashion of the body, arms and legs. Sometimes, however, the episodes are extensor (arching). Usually, they are symmetrical (affecting both sides equally) but sometimes one side is affected more than the other.
Typically, each episode lasts just one or two seconds, there is then a pause for a few seconds followed by a further spasm. While single spasms may happen, infantile spasms usually happen in ‘runs’ or ‘clusters’ of several in a row.
It is common for babies who have infantile spasms to become irritable and for their development to slow up or even to go backwards until the spasms are controlled. These infants can also behave as if they cannot see, but this improves once the spasms are controlled and the EEG has improved.
Diagnosis
The diagnosis of infantile spasms is made by a combination of the typical features with a typical EEG. The EEG shows a very disorganised pattern termed ‘hypsarrhythmia’. The EEG is always abnormal in children with West syndrome but sometimes this abnormality is seen only during sleep.
Infantile spasms, like many other ‘electroclinical syndromes’, have lots of different causes. A particular cause will be found in seven or eight children out of every 10 children with West syndrome.
Most children with infantile spasms will need a number of tests (EEG, brain scans, blood tests, urine tests and, sometimes, spinal fluid and other tests) in order to try to identify the underlying cause.
Treatment
The main treatments used are steroids or vigabatrin (Sabril), Nitrazepam and sodium valproate (Epilim), may also be used. The type of steroids used are prednisolone or tetracosactide. Steroids must be used carefully as this treatment may cause some unpleasant side effects.
Prognosis (outlook)
In some children, infantile spasms respond easily to treatment, whereas in others they remain very resistant. Most children unfortunately go on to have other kinds of seizures in later childhood including an epilepsy syndrome called the Lennox-Gastaut syndrome. Most children also have learning difficulties. The prognosis for infantile spasms in both these respects is largely dependent on the underlying cause of the condition.
Support organisations
West Syndrome Support Group, c/o Contact a Family, 209-211 City Road, London, EC1V 1JN, telephone 0808 808 3555, www.cafamily.org.uk
Contact a Family, 209-211 City Road, London, EC1V 1JN, telephone 0808 808 3555, www.cafamily.org.uk
Epilepsy Action is indebted to Dr Richard Appleton, a Consultant Paediatric Neurologist who specialises in children’s epilepsy, and to Dr Rachel Kneen, Consultant Paediatric Neurologist and Dr Stewart Macleod, Specialist Registrar in paediatric neurology, at Alder Hey at Alder Hey Children’s Hospital, Liverpool, who have kindly prepared this information.
Because this page is written by an epilepsy healthcare professional and not by Epilepsy Action, it falls outside the requirements of the Information Standard. This is why the Information Standard logo is not shown on this page.
This information is exempt under the terms of The Information Standard.
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Updated August 2009To be reviewed March 2012
Comments: read the 4 comments or add yours
Comments
My son was diagnosed as suffering from IS at 6 months old. We were lucky to have a great GP who recogised it straight away. We were admitted to hospital within 3 days of the first seizure. Sam was treated with prednesolone and his seizures stopped within 24hours. All in all he was in hospital for 10 days. He's now a bouncing 10 year old! He is a tiny bit behind at mainstream school but nothing to worry about. We were so lucky. Sam's diary was written for UKISS and hopefully more studies will be done to look into this horrid illness.
My son callam was diagnosed with is at 8months he was taking up to 20 spasms a day it was the most terrifying thing iv ever seen he spent 3 days in hospital then was transferd to one of the most amazing neurologist in the counrty Dr Zuberi at yorkhill they tryed him with steriods but they done nothing for him they gave him an eeg every week then put him on sabril and they stopped he still has the odd episode but hes now 18 months and started crawling and walking holding on to things his development is slow but he has 2 great big brothers and a big sister who encourage him to do things hes an insperation to me and im thankful that i have him hes just been diagnosed with astma as well and takes ill every few weeks but hes always laughing and smiling id just like to say that even with a child with is its not the end of the earth it just makes them even more special
Hello, anyone know about west syndrome? I have a nephew who has west syndrome. Which hospital could help us about therapy? Please reply on here ASAP. We are really wondering that!
Hi Deniz
Thanks for your comment.
For a hospital which could help, I would need to have some idea of where you live. Please feel free to contact us again, either by email or the Epilepsy Helpline freephone 0808 800 5050. Then we will be able to give you some specific hospital information.
In order to talk to other people who have or whose children have West syndrome you could join our online community for people with epilepsy and carers of people with epilepsy. It's called forum4e. Or you could go through Contact a Family. The details are at the bottom of our West syndrome webpage, but I have also linked you to them here.
Cherry
Advice and Information Team